Minoshima S - Search Results

1

Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome.

Matsuoka R, Kimura M, Scambler PJ, Morrow BE, Imamura S, Minoshima S, Shimizu N, Yamagishi H, Joh-o K, Watanabe S, Oyama K, Saji T, Ando M, Takao A, Momma K. Matsuoka R, et al. Among authors: minoshima s. Hum Genet. 1998 Jul;103(1):70-80. doi: 10.1007/s004390050786. Hum Genet. 1998. PMID: 9737780

2

Precise mapping of the EGF receptor gene on the human chromosome 7p12 using an improved fish technique.

Wang Y, Minoshima S, Shimizu N. Wang Y, et al. Among authors: minoshima s. Jpn J Hum Genet. 1993 Dec;38(4):399-406. doi: 10.1007/BF01907986. Jpn J Hum Genet. 1993. PMID: 8186417

3

Cot-1 banding of human chromosomes using fluorescence in situ hybridization with Cy3 labeling.

Wang Y, Minoshima S, Shimizu N. Wang Y, et al. Among authors: minoshima s. Jpn J Hum Genet. 1995 Sep;40(3):243-52. doi: 10.1007/BF01876182. Jpn J Hum Genet. 1995. PMID: 8527798

4

Role of TBX1 in human del22q11.2 syndrome.

Yagi H, Furutani Y, Hamada H, Sasaki T, Asakawa S, Minoshima S, Ichida F, Joo K, Kimura M, Imamura S, Kamatani N, Momma K, Takao A, Nakazawa M, Shimizu N, Matsuoka R. Yagi H, et al. Among authors: minoshima s. Lancet. 2003 Oct 25;362(9393):1366-73. doi: 10.1016/s0140-6736(03)14632-6. Lancet. 2003. PMID: 14585638

5

[Genetic information database].

Minoshima S, Shimizu N. Minoshima S, et al. Tanpakushitsu Kakusan Koso. 1996 Nov;41(15 Suppl):2464-77. Tanpakushitsu Kakusan Koso. 1996. PMID: 8952411 Review. Japanese. No abstract available.

6

[Genome information database].

Minoshima S, Shimizu N. Minoshima S, et al. Tanpakushitsu Kakusan Koso. 1997 Dec;42(17 Suppl):3038-45. Tanpakushitsu Kakusan Koso. 1997. PMID: 9455231 Review. Japanese. No abstract available.

7

Localization of the human AHNAK/desmoyokin gene (AHNAK) to chromosome band 11q12 by somatic cell hybrid analysis and fluorescence in situ hybridization.

Kudoh J, Wang Y, Minoshima S, Hashimoto T, Amagai M, Nishikawa T, Shtivelman E, Bishop JM, Shimizu N. Kudoh J, et al. Among authors: minoshima s. Cytogenet Cell Genet. 1995;70(3-4):218-20. doi: 10.1159/000134037. Cytogenet Cell Genet. 1995. PMID: 7789175

8

Mapping of the gene for human xanthine dehydrogenase (oxidase) (XDH) to band p23 of chromosome 2.

Minoshima S, Wang Y, Ichida K, Nishino T, Shimizu N. Minoshima S, et al. Cytogenet Cell Genet. 1995;68(1-2):52-3. doi: 10.1159/000133887. Cytogenet Cell Genet. 1995. PMID: 7956358 No abstract available.

9

[Analysis of disease-associated marker chromosomes using chromosome sorter].

Minoshima S, Shimizu N. Minoshima S, et al. Tanpakushitsu Kakusan Koso. 1996 Nov;41(15 Suppl):2174-81. Tanpakushitsu Kakusan Koso. 1996. PMID: 8952379 Review. Japanese. No abstract available.

10

[Computer softwares for DNA diagnosis: GeneViewPLUS and Mutation View].

Shimizu N, Minoshima S. Shimizu N, et al. Among authors: minoshima s. Rinsho Byori. 1997 Mar;45(3):209-12. Rinsho Byori. 1997. PMID: 9086822 Review. Japanese.

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